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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19842생성일: 2026년 10월 25일

4-Fluorobenzenesulfonyl chloride → (4,4-difluoropiperidin-1-yl)(1-(4-fluorophenylsulfonyl)-5-(1-isopropylpiperidin-4-yloxy)-1H-indol-2-yl)methanone

https://huagongshe.com/reaction/19842

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참여 물질

역할이름HCID투입량
반응물4-Fluorobenzenesulfonyl chlorideHCID 9588—
반응물Sodium hydrideHCID 24758—
반응물(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
용매DimethylformamideHCID 6228—
생성물(4,4-difluoropiperidin-1-yl)(1-(4-fluorophenylsulfonyl)-5-(1-isopropylpiperidin-4-yloxy)-1H-indol-2-yl)methanoneHCID 1673938760.1%

반응 조건

온도70 °C

반응 단계

Sodium hydride (60% dispersion in oil, 24 mg, 1.1 eq.) was added to a mixture of (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1, 200 mg, 1.0 eq.) in N,N-dimethylformamide (2 mL) and stirred at 70° C. for 30 min. 4-Fluorobenzenesulfonyl chloride (115 mg, 1.2 eq.) was added and the reaction mixture was stirred at 70° C. overnight. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate and the combined organic fractions were washed with water and brine, dried over sodium sulfate, filtered, evaporated to dryness and purified on silica gel, eluting with dichloromethane/methanol 49:1 to yield 167 mg (60%) of the desired product as yellow foam. MS (m/e): 564.4 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d19d1de50ed84a7a86192d66ab48a4da
출처 메모uspto-grants-2010_06